FOXQ1[gene] and "single gene"[properties] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2593017	NM_033260.4(FOXQ1):c.29C>A (p.Ala10Glu)	FOXQ1 (A10E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389567	NM_033260.4(FOXQ1):c.64G>A (p.Gly22Ser)	FOXQ1 (G22S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096580	NM_033260.4(FOXQ1):c.103G>A (p.Ala35Thr)	FOXQ1 (A35T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514153	NM_033260.4(FOXQ1):c.158C>T (p.Ala53Val)	FOXQ1 (A53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546118	NM_033260.4(FOXQ1):c.179C>T (p.Thr60Met)	FOXQ1 (T60M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299858	NM_033260.4(FOXQ1):c.181C>G (p.Gln61Glu)	FOXQ1 (Q61E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096582	NM_033260.4(FOXQ1):c.189C>A (p.Asp63Glu)	FOXQ1 (D63E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096583	NM_033260.4(FOXQ1):c.215C>A (p.Pro72Gln)	FOXQ1 (P72Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287058	NM_033260.4(FOXQ1):c.221C>T (p.Ala74Val)	FOXQ1 (A74V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409069	NM_033260.4(FOXQ1):c.290G>C (p.Gly97Ala)	FOXQ1 (G97A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656171	NM_033260.4(FOXQ1):c.302G>A (p.Gly101Asp)	FOXQ1 (G101D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2380041	NM_033260.4(FOXQ1):c.307G>A (p.Ala103Thr)	FOXQ1 (A103T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612023	NM_033260.4(FOXQ1):c.349C>T (p.Arg117Trp)	FOXQ1 (R117W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620454	NM_033260.4(FOXQ1):c.357G>C (p.Lys119Asn)	FOXQ1 (K119N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788530	NM_033260.4(FOXQ1):c.387C>T (p.Ala129=)	FOXQ1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3096585	NM_033260.4(FOXQ1):c.388A>C (p.Met130Leu)	FOXQ1 (M130L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096586	NM_033260.4(FOXQ1):c.430G>C (p.Glu144Gln)	FOXQ1 (E144Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096587	NM_033260.4(FOXQ1):c.550C>G (p.Pro184Ala)	FOXQ1 (P184A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 743235	NM_033260.4(FOXQ1):c.567C>T (p.Gly189=)	FOXQ1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096588	NM_033260.4(FOXQ1):c.616G>A (p.Asp206Asn)	FOXQ1 (D206N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388453	NM_033260.4(FOXQ1):c.689A>G (p.Glu230Gly)	FOXQ1 (E230G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096589	NM_033260.4(FOXQ1):c.692A>C (p.Glu231Ala)	FOXQ1 (E231A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388454	NM_033260.4(FOXQ1):c.698C>G (p.Pro233Arg)	FOXQ1 (P233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389954	NM_033260.4(FOXQ1):c.707C>T (p.Pro236Leu)	FOXQ1 (P236L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096590	NM_033260.4(FOXQ1):c.713C>T (p.Ala238Val)	FOXQ1 (A238V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328666	NM_033260.4(FOXQ1):c.737C>T (p.Pro246Leu)	FOXQ1 (P246L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540007	NM_033260.4(FOXQ1):c.786C>G (p.Ser262Arg)	FOXQ1 (S262R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284411	NM_033260.4(FOXQ1):c.853C>T (p.Arg285Cys)	FOXQ1 (R285C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312046	NM_033260.4(FOXQ1):c.872C>T (p.Pro291Leu)	FOXQ1 (P291L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610251	NM_033260.4(FOXQ1):c.874G>C (p.Gly292Arg)	FOXQ1 (G292R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319854	NM_033260.4(FOXQ1):c.898G>C (p.Ala300Pro)	FOXQ1 (A300P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319855	NM_033260.4(FOXQ1):c.899C>T (p.Ala300Val)	FOXQ1 (A300V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096591	NM_033260.4(FOXQ1):c.955G>A (p.Ala319Thr)	FOXQ1 (A319T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318474	NM_033260.4(FOXQ1):c.985G>A (p.Gly329Ser)	FOXQ1 (G329S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249707	NM_033260.4(FOXQ1):c.1001T>G (p.Leu334Arg)	FOXQ1 (L334R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768059	NM_033260.4(FOXQ1):c.1013A>G (p.Glu338Gly)	FOXQ1 (E338G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3096579	NM_033260.4(FOXQ1):c.1036C>T (p.Pro346Ser)	FOXQ1 (P346S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769313	NM_033260.4(FOXQ1):c.1041C>G (p.Pro347=)	FOXQ1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2351337	NM_033260.4(FOXQ1):c.1043T>C (p.Leu348Pro)	FOXQ1 (L348P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360291	NM_033260.4(FOXQ1):c.1061C>T (p.Pro354Leu)	FOXQ1 (P354L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302874	NM_033260.4(FOXQ1):c.1084C>T (p.Leu362Phe)	FOXQ1 (L362F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2408104	NM_033260.4(FOXQ1):c.1088G>C (p.Arg363Pro)	FOXQ1 (R363P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386299	NM_033260.4(FOXQ1):c.1097C>T (p.Ala366Val)	FOXQ1 (A366V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385321	NM_033260.4(FOXQ1):c.1120T>C (p.Cys374Arg)	FOXQ1 (C374R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365344	NM_033260.4(FOXQ1):c.1123C>T (p.Pro375Ser)	FOXQ1 (P375S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096581	NM_033260.4(FOXQ1):c.1171G>C (p.Gly391Arg)	FOXQ1 (G391R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213760	NM_033260.4(FOXQ1):c.1187A>C (p.Tyr396Ser)	FOXQ1 (Y396S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354176	NM_033260.4(FOXQ1):c.1201C>A (p.Leu401Ile)	FOXQ1 (L401I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 394187	GRCh37/hg19 6p25.3(chr6:1284030-1322348)x3	FOXQ1	Copy number gain	See cases	Gconflicting data from submitters
Select item 393819	GRCh37/hg19 6p25.3(chr6:1295851-1386995)x3	FOXQ1	Copy number gain	See cases	GLikely benign

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Items: 50